EP2136804A1 - Dérivés indolizine d'acide acétique utilisés comme antagonistes de crth2 - Google Patents

Dérivés indolizine d'acide acétique utilisés comme antagonistes de crth2

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Publication number
EP2136804A1
EP2136804A1 EP07732088A EP07732088A EP2136804A1 EP 2136804 A1 EP2136804 A1 EP 2136804A1 EP 07732088 A EP07732088 A EP 07732088A EP 07732088 A EP07732088 A EP 07732088A EP 2136804 A1 EP2136804 A1 EP 2136804A1
Authority
EP
European Patent Office
Prior art keywords
acetic acid
cyano
chloro
methylindolizin
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP07732088A
Other languages
German (de)
English (en)
Inventor
George Hynd
Nicholas Charles Ray
Harry Finch
John Gary Montana
Michael Colin Cramp
Trevor Keith Harrison
Rosa Arienzo
Paul Blaney
Yann Griffon
David Middlemiss
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pulmagen Therapeutics Asthma Ltd
Original Assignee
Argenta Oral Therapeutics Ltd
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Filing date
Publication date
Application filed by Argenta Oral Therapeutics Ltd filed Critical Argenta Oral Therapeutics Ltd
Publication of EP2136804A1 publication Critical patent/EP2136804A1/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/16—Central respiratory analeptics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents

Definitions

  • This invention relates to specific indolizine compounds which are ligands of the CRTH2 receptor (Chemoattractant Receptor-homologous molecule expressed on T Helper cells type 2), and their use in the treatment of diseases responsive to modulation of CRTH2 receptor activity, principally diseases having a significant inflammatory component.
  • CRTH2 receptor Cellular Receptor-homologous molecule expressed on T Helper cells type 2
  • Mast cells are known to play an important role in allergic and immune responses through the release of a number of mediators, such as histamine, leukotrienes, cytokines, prostaglandin D 2 , etc (Boyce; Allergy Asthma Proc, 2004, 25, 27-30).
  • Prostaglandin D 2 (PGD 2 ) is the major metabolite produced by the action of cyclooxygenase on arachadonic acid by mast cells in response to allergen challenge (Lewis et al; J. Immunol., 1982, 129, 1627-1631). It has been shown that PGD 2 production is increased in patients with systemic mastocytosis (Roberts; N. Engl. J.
  • PGD 2 mediates it effects through two receptors, the PGD 2 (or DP) receptor (Boie et al; J. Biol. Chem., 1995, 270, 18910-18916) and the chemoattractant receptor- homologous molecule expressed on Th2 (or CRTH2) (Nagata et al; J. Immunol., 1999, 162, 1278-1289; Powell; Prostaglandins Luekot. Essent. Fatty Acids, 2003, 69, 179-185). Therefore, it has been postulated that agents that antagonise the effects of PGD 2 at its receptors may have beneficial effects in a number of disease states.
  • the CRTH2 receptor has been shown to be expressed on cell types associated with allergic inflammation, such as basophils, eosinophils, and Th2-type immune helper cells (Hirai et al; J. Exp. Med., 2001 , 193, 255-261).
  • the CRTH2 receptor has been shown to mediate PGD 2 -mediated cell migration in these cell types (Hirai et al; J. Exp. Med., 2001 , 193, 255-261), and also to play a major role in neutrophil and eosinophil cell recruitment in a model of contact dermatitis (Takeshita et al; Int. Immunol., 2004, 16, 947-959).
  • R 1 , R 2 , R3 and R 4 each independently are hydrogen, CrC 6 alkyl, fully or partially fluorinated C r C 6 alkyl, halo, -S(O) n R 10 , -SO 2 N(R 10 ) 2 , -N(R 10 ) 2 , -C(O)N(R 10 ) 2 , - NR 10 C(O)R 9 , -CO 2 R 10 , -C(O)R 9 , -NO 2 , -CN Or -OR 11 ; wherein each R 9 is independently d-C ' ⁇ alkyl, aryl, heteroaryl;
  • R 10 is independently hydrogen, CrC 6 alkyl, aryl, or heteroaryl
  • Ri 1 is hydrogen, CrC 6 alkyl, fully or partially fluorinated C
  • n 0, 1 or 2;
  • R 5 is CrC 6 alkyl, fully or partially fluorinated C r C 6 alkyl, Ci-C 6 alkenyl, CrC 6 alkynyl, optionally substituted aryl, or optionally substituted heteroaryl;
  • R 6 is hydrogen, C r C 6 alkyl or fully or partially fluorinated d-C 6 alkyl;
  • R 7 and R 8 are independently hydrogen or Ci-C 6 alkyl, or R 7 and R 8 together with the atom to which they are attached form a cycloalkyl group; and
  • X is -CHR 6 -, -S(O) n -, -C(O)-, -NR 6 SO 2 - or -SO 2 NR 6 - wherein n is 0, 1 or 2.
  • the present invention provides a group of specific compounds falling within the scope of, but not specifically disclosed in our copending application PCT/GB2006/003394 referred to above.
  • the invention provides a compound selected from the group consisting of
  • Compounds with which the invention is concerned are CRTH2 receptor antagonists.
  • a second aspect of the invention is a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of the invention in admixture with a pharmaceutically acceptable carrier or excipient.
  • a third aspect of the invention is a compound of the invention for use in therapy.
  • a fourth aspect of the invention is the use of a compound of the invention in the manufacture of a medicament for the . treatment of a disease in which a CRTH2 antagonist can prevent, inhibit or ameliorate the pathology and/or symptomatology of the disease.
  • a fifth aspect of the invention is a method for treating a disease in a patient in which a CRTH2 antagonist can prevent, inhibit or ameliorate the pathology and/or symptomatology of the disease, which method comprises administering to the patient a therapeutically effective amount of a compound of the invention.
  • compounds with which the invention is concerned are useful in the treatment of disease associated with elevated levels of prostaglandin D2 (PGD2) or one or more active metabolites thereof.
  • PGD2 prostaglandin D2
  • diseases include asthma, rhinitis, allergic airway syndrome, allergic rhinobronchitis, bronchitis, chronic obstructive pulmonary disease (COPD), nasal polyposis, sarcoidosis, farmer ' s lung, fibroid lung, cystic fibrosis, chronic cough, conjunctivitis, atopic dermatitis, Alzheimer's disease, amyotrophic lateral sclerosis, AIDS dementia complex, Huntington's disease, frontotemporal dementia, Lewy body dementia, vascular dementia, Guillain-Barre syndrome, chronic demyelinating polyradiculoneurophathy, multifocal motor neuropathy, plexopathy, multiple sclerosis, encephalomyelitis, panencephalitis, cerebellar degeneration and encephalomyelitis, CNS trauma, migraine, stroke, rheumatoid arthritis, ankylosing spondylitis, Behget's Disease, bursitis, carpal tunnel syndrome, inflammatory bowel infections,
  • the compounds with which the invention is concerned are primarily of value for the treatment of asthma, chronic obstructive pulmonary disease, rhinitis, allergic airway syndrome, or allergic rhinobronchitis.
  • Psoriasis, atopic and non-atopic dermatitis Crohn's disease, ulcerative colitis, and irritable bowel disease are other specific conditions where.the present compounds may have particular utility.
  • salt includes base addition, acid addition and quaternary salts.
  • Compounds of the invention which are acidic can form salts, including pharmaceutically acceptable salts, with bases such as alkali metal hydroxides, e.g. sodium and potassium hydroxides; alkaline earth metal hydroxides e.g. calcium, barium and magnesium hydroxides; with organic bases e.g. N-methyl-D-glucamine, choline tris(hydroxymethyl)amino-methane, L-arginine, L-lysine, N-ethyl piperidine, dibenzylamine and the like.
  • bases such as alkali metal hydroxides, e.g. sodium and potassium hydroxides; alkaline earth metal hydroxides e.g. calcium, barium and magnesium hydroxides; with organic bases e.g. N-methyl-D-glucamine, choline tris(hydroxymethyl)amino-methane, L-arginine, L-lysine, N-ethyl pipe
  • Specific salts with bases include the benzathine, calcium, diolamine, meglumine, olamine, potassium, procaine, sodium, tromethamine and zinc salts.
  • Those compounds of the invention which are basic can form salts, including pharmaceutically acceptable salts with inorganic acids, e.g. with hydrohalic acids such as hydrochloric or hydrobromic acids, sulphuric acid, nitric acid or phosphoric acid and the like, and with organic acids e.g.
  • acceptable counter-ions may be, for example, chlorides, bromides, sulfates, methanesulfonates, benzenesulfonates, toluenesulfonates (tosylates), napadisylates (naphthalene- 1 ,5-disulfonates or naphthalene-1 -(sulfonic acid)-5-sulfonates), edisylates (ethane-1 ,2-disulfonates or ethane-1 -(sulfonic acid)-2-sulfonates), isethionates (2-hydroxyethylsulfonates), phosphates, acetates, citrates, lactates, tartrates, mesylates, maleates, malates, fumarates, succinates, xinafoates, p- acetamidobenzoates and the like; where
  • prodrugs such as esters
  • Prodrug means a compound which is convertible in vivo by metabolic means (e.g. by hydrolysis, reduction or oxidation) to a compound of formula (I).
  • metabolic means e.g. by hydrolysis, reduction or oxidation
  • an ester prodrug of a compound of formula (I) may be convertible by hydrolysis in vivo to the parent molecule.
  • esters of compounds of formula (I) are for example acetates, citrates, lactates, tartrates, malonates, oxalates, salicylates, propionates, succinates, fumarates, maleates, methylene-bis- ⁇ -hydroxynaphthoates, gentisates, isethionates, di-p-toluoyltartrates, methanesulphonates, ethanesulphonates, benzenesulphonat.es, p-toluene- sulphonates, cyclohexylsulphamates and quinates.
  • ester prodrugs are those described by F. J. Leinweber, Drug Metab. Res., 1987, 18, 379. As used in herein, references to the compounds of formula (I) are meant to also include the prodrug forms.
  • the compounds with which the invention is concerned are CRTH2 receptor antagonists, and are useful in the treatment of diseases which benefit from such modulation.
  • diseases which benefit from such modulation. Examples of such diseases are referred to above, and include asthma, rhinitis, allergic airway syndrome, and allergic rhinobronchitis.
  • the specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug combination and the severity of the particular disease undergoing treatment. Optimum dose levels and frequency of dosing will be determined by clinical trial, as is required in the pharmaceutical art. In general, the daily dose range will lie within the range of from about 0.001 mg to about 100 mg per kg body weight of a mammal, often 0.01 mg to about 50 mg per kg, for example 0.1 to 10 mg per kg, in single or divided doses. On the other hand, it may be necessary to use dosages outside these limits in some cases.
  • compositions may be in the form of tablets, capsules, powders, granules, lozenges, liquid or gel preparations, such as oral, topical, or sterile parenteral solutions or suspensions.
  • Tablets and capsules for oral administration may be in unit dose presentation form, and may contain conventional excipients such as binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers for example lactose, sugar, maize-starch, calcium phosphate, sorbitol or glycine; tabletting lubricant, for example magnesium stearate, talc, polyethylene glycol or silica; disintegrants for example potato starch, or acceptable wetting agents such as sodium lauryl sulphate.
  • the tablets may be coated according to methods well known in normal pharmaceutical practice.
  • Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for reconstitution with water or other suitable vehicle before use.
  • Such liquid preparations may contain conventional additives such as suspending agents, for example sorbitol, syrup, methyl cellulose, glucose syrup, gelatin hydrogenated edible fats; emulsifying agents, for example lecithin, sorbitan monooleate, or acacia; non-aqueous vehicles (which may include edible oils), for example almond oil, fractionated coconut oil, oily esters such as glycerine, propylene glycol, or ethyl alcohol; preservatives, for example methyl or propyl p-hydroxybenzoate or sorbic acid, and if desired conventional flavourin ⁇ or colourin ⁇ a ⁇ ents.
  • suspending agents for example sorbitol, syrup, methyl cellulose, glucose syrup, gelatin hydrogenated edible fats
  • emulsifying agents for example lecithin, sorbitan monooleate, or acacia
  • non-aqueous vehicles which may include edible oils
  • almond oil fractionated coconut oil
  • oily esters such as gly
  • the drug may be made up into a cream, lotion or ointment.
  • Cream or ointment formulations which may be used for the drug are conventional formulations well known in the art, for example as described in standard textbooks of pharmaceutics such as the British Pharmacopoeia.
  • the drug may also be formulated for inhalation, for example as a nasal spray, or dry powder or aerosol inhalers.
  • the active compound is preferably in the form of microparticles. They may be prepared by a variety of techniques, including spray-drying, freeze-drying and micronisation. Aerosol generation can be carried out using, for example, pressure-driven jet atomizers or ultrasonic atomizers, preferably using propellant-driven metered aerosols or propellant-free administration of micronized active compounds from, for example, inhalation capsules or other "dry powder" delivery systems.
  • the active ingredient may also be administered parenterally in a sterile medium.
  • the drug can either be suspended or dissolved in the vehicle.
  • adjuvants such as a local anaesthetic, preservative and buffering agents can be dissolved in the vehicle.
  • compositions for preventing and treating PGD 2 -mediated diseases comprising a therapeutically effective amount of a compound of the invention and one or more other therapeutic agents.
  • Suitable therapeutic agents for a combination therapy with compounds of the invention include, but are not limited to: (1) corticosteroids, such as fluticasone, budesonide or ciclesonide; (2) ⁇ 2-adrenoreceptor agonists, such as salmeterol, formeterol or indacaterol; (3) leukotriene modulators, for example leukotriene antagonists such as montelukast or pranlukast or leukotriene biosynthesis inhibitors such as Zileuton or BAY-x1005; (4) anticholinergic agents, for example muscarinic-3 (M 3 ) receptor antagonists such as tiotropium bromide; (5) phosphodiesterase-IV (PDE-IV) inhibitors, such as roflumilast or cilomilast; (6) antihistamines, for example selective histamine-1 (H1) receptor antagonists, such as loratidine or astemizole; (7) antitussive agents, such as codeine
  • the weight ratio of the compound of the invention to the second active ingredient may be varied and will depend upon the effective dose of each ingredient. Generally, an effective dose of each will be used.
  • Mass Spectrometry (LCMS) experiments to determine retention times and associated mass ions were performed using the following methods: Method A: experiments were performed on a Micromass Platform LCT spectrometer with positive ion electrospray and single wavelength UV 254 nm detection using a Higgins Clipeus C18 5 ⁇ m 100 x 3.0 mm column and a 2 ml_ / minute flow rate.
  • the initial solvent system was 95 % water containing 0.1 % formic acid (solvent A) and 5 % acetonitrile containing 0.1 % formic acid (solvent B) for the first minute followed by a gradient up to 5 % solvent A and 95 % solvent B over the next 14 minutes.
  • the final solvent system was held constant for a further 2 minutes.
  • Method B experiments were performed on a Micromass Platform LC spectrometer with positive and negative ion electrospray and ELS / Diode array detection using a Phenomenex Luna C18(2) 3O x 4.6 mm column and a 2 mL / minute flow rate.
  • the solvent system was 95 % solvent A and 5 % solvent B for the first 0.50 minutes followed by a gradient up to 5 % solvent A and 95 % solvent B over the next 4 minutes. The final solvent system was held constant for a further 0.50 minutes
  • Method C experiments were performed on a Agilent Scalar column C18, 5 ⁇ m (4.6 x 50 mm, flow rate 2.5 mL / minute) eluting with a H 2 CVMeCN gradient containing 0.1 % v/v formic acid over 7 minutes with UV detection at 215 and 254 nm.
  • Method D experiments were performed on a Agilent Scalar column C18, 5 ⁇ m (4.6 x 50 mm, flow rate 2.5 mL / minutes) eluting with a H 2 O / MeCN gradient containing 0.1 % v/v NH 4 OH over 7 minutes with UV detection at 215 and 254 nm.
  • Preparation 1e acetic acid acetoxy[4-(morpholine-4-sulfonyl)phenyl]methyl ester
  • a solution of morpholine (0.85 ml_) in dichloromethane (5.0 mL) was added dropwise to a mixture of acetic acid acetoxy(4-chlorosulfonylphenyl)methyl ester (1.0 g) and dichloromethane (25 mL) at 0 0 C and the resulting mixture was stirred at room temperature overnight.
  • the title compound was prepared by the method of Preparation 1g using (7-cyano- 2-methylindolizin-3-yl)acetic acid ethyl ester and 3-chloro-4- ethanesulfonylbenzaldehyde.
  • Example 3 ⁇ 1 -[3-chloro-4-(morpholine-4-sulf onyl)benzyl]-7-cyano-2- methylindolizin-3-yl ⁇ acetic acid
  • the title compound was prepared by the method of Preparation 1g using (7-cyano- 2-methylindolizin-3-yl)acetic acid ethyl ester and 3-chloro-4-(morpholine-4- sulfonyl)benzaldehyde.
  • the title compound was prepared by the method of Preparation 4b using 4-(2- chloro-4-fluorobenzenesulfonyl)morpholine.
  • Preparation 5c ⁇ 1 -[3-chloro-4-(morpholine-4-sulfonyl)phenylsulfanyl]-7-cyano-2- methylindolizin-3-yl ⁇ acetic acid ethyl ester
  • the title compound was prepared by the method of Preparation 4c using (7-cyano-2- methylindolizin-3-yi)acetic acid ethyl ester and bis(3-chloro-4- morpholinosulfonylbenzene)disulfide.
  • Radioligand Binding Assay The receptor binding assay is performed in a final volume of 200 ⁇ l_ binding buffer [10 mM BES (pH 7.4), 1 mM EDTA, 10 mM manganese chloride, 0.01 % BSA] and 1 nM [ 3 H]-PGD 2 (Amersham Biosciences UK Ltd). Ligands are added in assay buffer containing a constant amount of DMSO (1 % by volume). Total binding is determined using 1 % by volume of DMSO in assay buffer and non-specific binding is determined using 10 ⁇ M of unlabeled PGD 2 (Sigma).
  • HEK Human embryonic kidney
  • HEK cell membranes 3.5 ⁇ g expressing the CRTH2 receptor are incubated with 1.5 mg wheatgerm agglutinin SPA beads and 1 nM [ 3 H]-PGD 2 (Amersham Biosciences UK Ltd) and the mixture incubated for 3 hours at room temperature.
  • Bound [ 3 H]-PGD 2 is detected using a Microbeta TRILUX liquid scintillation counter (Perkin Elmer).
  • Compound IC 50 value is determined using a 6-point dose response curve in duplicate with a semi-log compound dilution series. IC 50 calculations are performed using Excel and XLfit (Microsoft), and this value is used to determine a Ki value for the test compound using the Cheng-Prusoff equation.
  • the GTP ⁇ S Assay is performed in a final volume of 200 mL assay buffer (2OmM HEPES pH 7.4, 1OmM MgCI 2 , 10OmM NaCI, 10 ⁇ g/mL saponin). DMSO concentrations are kept constant at 1% by volume.
  • Human embryonic kidney (HEK) cell membranes (3.5 ⁇ g) expressing the CRTH2 receptor are incubated with the compounds for 15 min at 30° C prior to addition of PGD 2 (3OnM final concentration) and GTP (10 ⁇ M final concentration).
  • the assay solutions are then incubated for 30 minutes at 30° C, followed by addition of [ 35 S]-GTP ⁇ S (0.1 nM final concentration).
  • the assay plate is than shaken and incubated for 5 minutes at 30°C.
  • SPA beads (Amersham Biosciences, UK) are added to a final concentration of 1.5mg/well and the plate shaken and incubated for 30 minute at 30° C.
  • the sealed plate is centrifuged at 1000g for IOmins at 30oC and the bound [ 35 S]-GTP ⁇ S is detected on Microbeta scintillation counter (Perkin Elmer).
  • Compound IC 50 value is determined using a 6-point dose response curve in duplicate with a semi-log compound dilution series. IC 50 calculations are performed using Excel and XLfit (Microsoft), and this value is used to determine a Ki value for the test compound using the Cheng-Prusoff equation.
  • the compounds of the Examples above were tested in the CRTH2 radioligand binding and GTP ⁇ S functional assays described above; the compounds all have IC 50 values of less than 1 ⁇ M in both assays.
  • the compound of Example 1 had an IC 50 value of 58 nM in the CRTH2 radioligand binding assay, and the compound of Example 6 had an IC 50 value of 19 nM in that assay..

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  • Pulmonology (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

L'invention concerne les composés spécifiques de la liste suivante : acide {7-cyano-2-méthyl-1-[4-(morpholine-4-sulfonyl)benzyl]indolizin-3-yl}acétique, acide {1 -(3-chloro-4-éthanesulfonylbenzyl)-7-cyano-2-méthylindolizin-3-yl}acétique, acide {1-[3-chloro4-(morpholine-4-sulfonyl)benzyl]-7-cyano-2-méthylindolizin-3-yl}acétique, acide {1-(3-chloro-4-éthanesulfonylphénylsulfanyl)-7-cyano-2-méthylindolizin-3-yl}acétique, acide {1-[3-chloro-4-(morpholine-4-sulfonyl)phénylsulfanyl]-7-cyano-2-méthylindolizin-3- yl}acétique, acide {7-cyano-1 -(6-fluoroquinolin-2-ylméthyl)-2-méthylindolizin-3-yl}acétique, lesdits composés étant des ligands du récepteur CRTh2 et se révélant utiles dans le traitement des maladies respiratoires.
EP07732088A 2007-03-21 2007-03-21 Dérivés indolizine d'acide acétique utilisés comme antagonistes de crth2 Withdrawn EP2136804A1 (fr)

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PCT/GB2007/000996 WO2008113965A1 (fr) 2007-03-21 2007-03-21 Dérivés indolizine d'acide acétique utilisés comme antagonistes de crth2

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US (1) US20100137300A1 (fr)
EP (1) EP2136804A1 (fr)
JP (1) JP2010522149A (fr)
CN (1) CN101678009A (fr)
AU (1) AU2007349641A1 (fr)
BR (1) BRPI0721477A2 (fr)
CA (1) CA2681409A1 (fr)
EA (1) EA200970875A1 (fr)
IL (1) IL201090A0 (fr)
MX (1) MX2009010068A (fr)
NO (1) NO20093039L (fr)
WO (1) WO2008113965A1 (fr)

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Publication number Priority date Publication date Assignee Title
GB0719485D0 (en) * 2007-10-05 2007-11-14 Argenta Discovery Ltd Compounds
DK2229358T3 (da) 2007-12-14 2011-07-04 Pulmagen Therapeutics Asthma Ltd Indoler og deres terapeutiske anvendelse
SI2558447T1 (sl) 2010-03-22 2015-01-30 Actelion Pharmaceuticals Ltd. Derivati 3-(heteroaril-amino)-1,2,3,4-tetrahidro-9h-karbazola in njihova uporaba kot modulatorji prostaglandinskega receptorja d2
EP2457900A1 (fr) 2010-11-25 2012-05-30 Almirall, S.A. Nouveaux dérivés de pyrazole présentant un comportement antagoniste CRTH2
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MX2009010068A (es) 2010-02-24
EA200970875A1 (ru) 2010-04-30
CN101678009A (zh) 2010-03-24
IL201090A0 (en) 2010-05-17
NO20093039L (no) 2009-11-17
US20100137300A1 (en) 2010-06-03
WO2008113965A1 (fr) 2008-09-25
AU2007349641A1 (en) 2008-09-25
BRPI0721477A2 (pt) 2013-01-15
JP2010522149A (ja) 2010-07-01

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